Canonical Allele Identifier: CA377670582
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780580A>C , CM000672.2:g.94780580A>C GRCh38
NC_000010.10:g.96540337A>C , CM000672.1:g.96540337A>C GRCh37
NC_000010.9:g.96530327A>C NCBI36
NG_008384.2:g.22875A>C
NG_008384.3:g.22900A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.563A>C MANE Select ENSP00000360372.3:p.Asp188Ala
ENST00000645461.1:n.1616A>C
ENST00000371321.7:c.563A>C ENSP00000360372.3:p.Asp188Ala
ENST00000464755.1:c.1326A>C ENSP00000483243.1:n.1326A>C
NM_000769.2:c.563A>C NP_000760.1:p.Asp188Ala
NM_000769.4:c.563A>C MANE Select NP_000760.1:p.Asp188Ala